441285-17-2 Usage
General Description
2-(3-(benzyloxycarbonyl)phenyl)acetic acid, also known as Boc-phenylacetic acid, is a compound commonly used in organic synthesis and pharmaceutical research. Its chemical structure consists of a phenylacetic acid core with a benzyloxycarbonyl (Boc) protecting group attached at the third position of the phenyl ring. This protecting group is commonly used to temporarily block reactive sites in organic synthesis, and can be removed under mild reaction conditions. Boc-phenylacetic acid has potential applications in the development of pharmaceuticals and agrochemicals, as well as in the synthesis of complex organic molecules. Its versatile reactivity and structural flexibility make it a valuable building block in chemical research and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 441285-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,2,8 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 441285-17:
(8*4)+(7*4)+(6*1)+(5*2)+(4*8)+(3*5)+(2*1)+(1*7)=132
132 % 10 = 2
So 441285-17-2 is a valid CAS Registry Number.
441285-17-2Relevant articles and documents
NOVEL BETA 3 ADRENERGIC RECEPTOR AGONISTS
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Page/Page column 29, (2011/11/13)
The present invention provides compounds of Formula (I), pharmaceutical compositions thereof, and methods of using the same in the treatment or prevention of diseases mediated by the activation of b3-adrenoceptor.
HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS
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Page/Page column 18, (2009/10/17)
The present invention provides compounds of Formula (I), pharmaceutical compositions thereof, and method of using the same in the treatment or prevention of diseases mediated by the activation of β3-adrenoceptor.
Design of novel antibiotics that bind to the ribosomal acyltransfer site
Haddad, Jalal,Kotra, Lakshmi P.,Llano-Sotelo, Beatriz,Kim, Choonkeun,Azucena Jr., Eduardo F.,Liu, Meizheng,Vakulenko, Sergei B.,Chow, Christine S.,Mobashery, Shahriar
, p. 3229 - 3237 (2007/10/03)
The structure of neamine bound to the A site of the bacterial ribosomal RNA was used in the design of novel aminoglycosides. The design took into account stereo and electronic contributions to interactions between RNA and aminoglycosides, as well as a ran
